Variant #0001014201 (NC_000006.11:g.31915199G>A, NM_006929.4:c.-11771G>A (SKIV2L))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31915199G>A
DNA change (hg38) -
Published as CFB(NM_001710.6):c.559G>A (p.V187I)
ISCN -
DB-ID C2_000068 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 3.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 ?/. - c.*2065G>A r.(=) p.(=)
CFB NM_001710.5 ?/. - c.559G>A r.(?) p.(Val187Ile)
NELFE NM_002904.5 ?/. - c.*4879C>T r.(=) p.(=)
SKIV2L NM_006929.4 ?/. - c.-11771G>A r.(?) p.(=)
ZBTB12 NM_181842.2 ?/. - c.-45606C>T r.(?) p.(=)


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